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• Wrs
  {{PAGENAME}} - human kcnq1 wild type allele is located in the vicinity of 11p15.5 and is approximately 404 kb in length. This allele, which encodes potassium
  516 bytes (71 words) - 14:13, 6 April 2024
• Silver-Russell syndrome
  ...a hypomethylation of the imprinting control region 1 (ICR1) on chromosome 11p15.5. Additionally, maternal uniparental disomy of chromosome 7 (mUPD7) is found ...etic testing can confirm a diagnosis by identifying hypomethylation of the 11p15.5 region or maternal uniparental disomy of chromosome 7.
  3 KB (415 words) - 03:42, 23 March 2024
• SLC22A18
  ...te carrier family 22 member 18''' gene. This gene is located on chromosome 11p15.5, a region which is associated with [[Beckwith-Wiedemann syndrome]], [[Wilms
  1 KB (214 words) - 05:56, 10 March 2024
• Transaldolase deficiency
  The disorder is caused by mutations in the '''transaldolase gene (TALDO1, 11p15.5-p15.4)'''.
  2 KB (246 words) - 18:09, 10 December 2020
• Culler–Jones syndrome
  ...caused by mutations in the ''CDKN1C'' gene, which is located on chromosome 11p15.5. This gene is an important regulator of cell proliferation, and its dysfunc
  2 KB (331 words) - 16:05, 30 March 2024
• Interferon-induced transmembrane protein 5
  ...gene is located on the short arm of the Crick strand of [[chromosome 11]] (11p15.5). It is located with a cluster of [[interferon]] inducible genes but is its
  2 KB (289 words) - 05:41, 24 February 2024
• Mucin 5B
  The ''MUC5B'' gene is located on the long arm of chromosome 11 (11p15.5). Variants in the ''MUC5B'' promoter region have been associated with both
  3 KB (375 words) - 12:27, 21 March 2024
• Exomphalos-macroglossia-gigantism syndrome
  ...in the regulation of gene expression in a region of chromosome 11 known as 11p15.5. This region contains several genes that are critical for growth and develo
  3 KB (380 words) - 15:28, 30 March 2024
• Gene imprinting
  ...A growth disorder often caused by misregulation of imprinted genes in the 11p15.5 region.
  3 KB (460 words) - 06:24, 28 March 2024
• Sirtuin 3
  The gene encoding SIRT3 is located on human chromosome 11p15.5. Variants within or near the SIRT3 gene have been studied for their associa
  3 KB (422 words) - 03:58, 22 March 2024
• Human β-globin locus
  The human β-globin locus is located on the short arm of chromosome 11 (11p15.5). It spans approximately 60 kilobases (kb) and includes five genes in the o
  3 KB (446 words) - 05:42, 31 March 2024
• Cyclin-dependent kinase inhibitor 1C
  ...ene is located on the short (p) arm of [[chromosome 11]] at position 15.5 (11p15.5), within a region implicated in several genetic disorders and cancers. The
  3 KB (447 words) - 06:13, 19 March 2024
• Cathepsin D
  The ''CTSD'' gene is located on [[chromosome 11]] (11p15.5) in humans. Mutations in this gene can lead to altered enzyme activity or s
  3 KB (432 words) - 18:43, 27 March 2024
• HBB
  ...the short (p) arm of [[chromosome 11]] at position 15.5, more precisely at 11p15.5. The gene spans approximately 1.6 kilobases and consists of three exons and
  4 KB (555 words) - 19:31, 22 March 2024
• Freeman–Sheldon syndrome
  ...Quinn JR, Bohnsack JF |title=A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter |journal=[[Am. J. Hum. Genet.]] |volume=60 |issue=2 |pages=426–32 |y
  21 KB (2,650 words) - 15:05, 9 September 2020
• Medical-dictionary-0-9
  * [[11p15.5 p15.4]]
  14 KB (1,362 words) - 02:37, 5 November 2023
• Long QT syndrome
  51 KB (7,085 words) - 15:34, 1 May 2020